Electrophoretic mobility capillary electrophoresis

All these methods benefit from the different behavior of free vs. bound substrate. Association involves changes of molecular size and/or charge, which controls electrophoretic mobility. Capillary electrophoresis provides mobility data as well as analytical concentrations with a minimal consumption of substances. During the past decade a variety of methods have been developed using mobility data or direct concentration readings from the detector to get information on the association constants (2-4). 

Separation by electrophoresis is based on differences in analyte velocity in an applied electric field within the capillary. The electrophoretic mobility of the analyte (ji ) depends on the characteristics of the analyte (electrical charge, molecular size, and shape) and the characteristics of the running buffer (type and ionic strength of the electrolyte, pH, viscosity, and properties of the additives) in which the migration takes place [1-3]. 

First, solutes with larger electrophoretic mobilities (in the same direction as the electroosmotic flow) have greater efficiencies thus, smaller, more highly charged solutes are not only the first solutes to elute, but do so with greater efficiency. Second, efficiency in capillary electrophoresis is independent of the capillary s length. Typical theoretical plate counts are approximately 100,000-200,000 for capillary electrophoresis. 

A form of capillary electrophoresis in which separations are based on differences in the solutes electrophoretic mobilities. 

Electroosmotic flow in a capillary also makes it possible to analyze both cations and anions in the same sample. The only requirement is that the electroosmotic flow downstream is of a greater magnitude than electrophoresis of the oppositely charged ions upstream. Electro osmosis is the preferred method of generating flow in the capillary, because the variation in the flow profile occurs within a fraction of Kr from the wall (49). When electro osmosis is used for sample injection, differing amounts of analyte can be found between the sample in the capillary and the uninjected sample, because of different electrophoretic mobilities of analytes (50). Two other methods of generating flow are with gravity or with a pump. 

Williams, B. A. and Vigh, G., Effect of the initial potential ramp on the accuracy of electrophoretic mobilities in capillary electrophoresis, Anal. Chem., 67, 3079, 1995. 

Grossman, P. D., Colburn, J. C., and Lauer, H. H., A semiempirical model for the electrophoretic mobilities of peptides in tree-solution capillary electrophoresis, Anal. Biochem., 179, 28, 1989. 

Rickard, E. C., Strohl, M. M., and Nielsen, R. G., Correlation of electrophoretic mobilities from capillary electrophoresis with physicochemical properties of proteins and peptides, Anal. Biochem., 197, 197, 1991. 

McKillop, A.G., Smith, R.M., Rowe, R.C., and Wren, S.A.C., Modeling and prediction of electrophoretic mobilities in capillary electrophoresis separation of alkylpyridines, Anal. Chem. 71, 497, 1999. 

Capillary zone electrophoresis, an up-to-date high resolution separation method useful for proteins and peptides, has been shown to be a useful method for determining electrophoretic mobilities and diffusion coefficients of proteins [3], Diffusion coefficients can be measured from peak widths of analyte bands. The validity of the method was demonstrated by measuring the diffusion coefficients for dansylated amino acids and myoglobin. 

Y Walbroehl, J Jorgenson. Capillary zone electrophoresis for determination of electrophoretic mobilities and diffusion coefficients. J Microcolumn Separ 1 41, 1989. 

Karim, M.R., Shinagawa, S., Takagi, T. (1994). Electrophoretic mobilities of the complexes between sodium dodecyl sulfate and various peptides or proteins determined by free solution electrophoresis using coated capillaries. Electrophoresis 15, 1141-1146. 

Capillary electrophoresis (CE) is a modem analytical technique that allows the rapid and efficient separation of sample components based on differences in their electrophoretic mobilities as they migrate or move through narrow bore capillary tubes (Frazier et al., 2000a). While widely accepted in the pharmaceutical industry, the uptake of CE by food analysts has been slow due to the lack of literature dedicated to its application in food analysis and the absence of well-validated analytical procedures applicable to a broad range of food products. 

Anions and uncharged analytes tend to spend more time in the buffered solution and as a result their movement relates to this. While these are useful generalizations, various factors contribute to the migration order of the analytes. These include the anionic or cationic nature of the surfactant, the influence of electroendosmosis, the properties of the buffer, the contributions of electrostatic versus hydrophobic interactions and the electrophoretic mobility of the native analyte. In addition, organic modifiers, e.g. methanol, acetonitrile and tetrahydrofuran are used to enhance separations and these increase the affinity of the more hydrophobic analytes for the liquid rather than the micellar phase. The effect of chirality of the analyte on its interaction with the micelles is utilized to separate enantiomers that either are already present in a sample or have been chemically produced. Such pre-capillary derivatization has been used to produce chiral amino acids for capillary electrophoresis. An alternative approach to chiral separations is the incorporation of additives such as cyclodextrins in the buffer solution. 

This is a more recently developed technique which is a hybrid between HPLC and capillary electrophoresis. The capillary is packed with HPLC media and the mobile phases are aqueous buffers. A voltage is applied to generate an electroendosmotic flow and the analytes separate by interaction with the stationary phase and electrophoretic forces no pump being required as for HPLC. Improved separation efficiencies have been reported. 

In CZE, the capillary, inlet reservoir, and outlet reservoir are filled with the same electrolyte solution. This solution is variously termed background electrolyte, analysis buffer, or run buffer. In CZE, the sample is injected at the inlet end of the capillary, and components migrate toward the detection point according to their mass-to-charge ratio by the electrophoretic mobility and separations principles outlined in the preceding text. It is the simplest form of CE and the most widely used, particularly for protein separations. CZE is described in Capillary Zone Electrophoresis. ... 

Electrophoretic injection can be used as a means for zone sharpening or sample concentration if the amount of ions, particularly salt or buffer ions, is lower in the sample than the running buffer. Because sample ions enter the capillary based on mobility, low-mobility ions will be loaded to a lesser extent than high-mobility ions. For this reason, the presence of nonsample ions will reduce injection efficiency, so electrophoretic injection is very sensitive to the presence of salts or buffers in the sample matrix. The disadvantages of electrophoretic injection argue against its use in routine analysis except in cases where displacement injection is not possible, e.g., in capillary gel electrophoresis (CGE) or when sample concentration by stacking is necessary. 

Affinity capillary electrophoresis (ACE), reviewed by Shimura and Kasai,42 is a method for studying receptor-ligand binding in free solution using CE. The technique depends upon a shift in the electrophoretic mobility of the receptor upon complexation with a charged ligand. Pure receptor preparations or accurate concentration values are not required because only migration times are measured. 

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